{"Aliases":["Schembl49158","Chembl2104874","Phenyl(2-piperidinyl)methyl acetate #","1-Phenyl-1-(2'-piperidyl)-1-acetoxymethane"],"ChemicalClasses":["2-benzylpiperidine"],"Chirality":"racemic","Classes":["Stimulant"],"EliminationHalfLife":"","Erowid Experience Reports":[],"Esters":[],"Formating":[],"HeavyAtomCount":17,"IUPACName":"[phenyl(piperidin-2-yl)methyl] acetate","InChI":"InChI=1S/C14H19NO2/c1-11(16)17-14(12-7-3-2-4-8-12)13-9-5-6-10-15-13/h2-4,7-8,13-15H,5-6,9-10H2,1H3","InChIKey":"BKPLVPRTTWIDNL-UHFFFAOYSA-N","MeSH Headers":[],"MolecularFormula":"C\u003csub\u003e14\u003c/sub\u003eH\u003csub\u003e19\u003c/sub\u003eNO\u003csub\u003e2\u003c/sub\u003e","MolecularWeight":"233.31 g/mol","PubChemId":558526,"RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Levophacetoperane","Name":"Phacetoperane","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/558526","Name":"Phacetoperane","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 558526, Phacetoperane. Accessed May 8, 2026. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/558526\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/558526\u003c/a\u003e","Anvisa. RDC Nº 784 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial. Diário Oficial da União. March 31, 2023. Accessed May 8, 2026. \u003ca href=https://www.in.gov.br/en/web/dou/-/resolucao-rdc-n-784-de-31-de-marco-de-2023-474904992\u003ehttps://www.in.gov.br/en/web/dou/-/resolucao-rdc-n-784-de-31-de-marco-de-2023-474904992\u003c/a\u003e"],"SMILES":"CC(=O)OC(C1CCCCN1)C2=CC=CC=C2","SaltData":[],"Salts":[],"Scheduling":[{"gov":"Brazil","ref":["2"],"schedule":"C1 substance"}],"StereoisomerData":[{"SMILES":"CC(=O)O[C@@H](C1=CC=CC=C1)[C@@H]1CCCCN1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.29 70.535\"\u003e\u003crect width=\"100%\" height=\"100%\" fill=\"#fff\"/\u003e\u003cdesc\u003eGenerated by the Chemistry Development Kit (http://github.com/cdk)\u003c/desc\u003e\u003cg fill=\"#ff0d0d\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h82v71H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m27.447.91-.003 15.24\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m28.663 16.854-10.53 6.078M27.445 14.742 16.914 20.82\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m18.133 22.932 5.265-3.039M16.914 20.82l5.266-3.039\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.444 16.15 9.914 5.726\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M40.289 39.012h.7M39.998 36.472h1.283M39.706 33.932h1.867M39.415 31.392h2.45M39.124 28.852h3.033\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M41.865 31.392H40.64M42.157 28.852h-1.516\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.639 39.012-13.2 7.618\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M27.439 46.63 14.238 39M25.001 48.037l-10.764-6.222\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.238 39-13.2 7.617\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 46.617.003 15.249M3.477 48.025l.002 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.041 61.866 13.201 7.63\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.242 69.496 13.2-7.617M14.243 66.681l10.76-6.21\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.439 46.63.003 15.249M40.639 39.012l13.197 7.622M53.836 46.634v15.24M53.836 61.874l13.208 7.62M67.044 69.494l13.208-7.62M80.252 61.874v-15.24M80.252 46.634l-10.055-5.8\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"m53.661 46.331.35.607 10.72-4.647-.841-1.457-.84-1.458z\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M16.504 23.765q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.31.25-.565.756-.881.506-.315 1.274-.315.732 0 1.232.315.5.31.756.875.256.566.256 1.328m-3.863 0q0 .923.387 1.459.392.529 1.22.529.839 0 1.22-.529.387-.536.387-1.459 0-.929-.387-1.453-.381-.523-1.208-.523-.834 0-1.227.523-.392.524-.392 1.453M42.901 23.769q0 .756-.256 1.328-.256.565-.756.881-.501.315-1.245.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.881t1.274-.316q.732 0 1.233.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.22.53.84 0 1.221-.53.387-.536.387-1.459 0-.928-.387-1.452-.381-.524-1.209-.524-.833 0-1.226.524t-.393 1.452\" class=\"atom\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.985 41.464h-.721l-2.619-4.066h-.03l.03.595q.024.358.024.733v2.738h-.566v-4.899h.715l2.607 4.054h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.768h.578zM68.848 36.003h-.619v-2.286h-2.513v2.286h-.613v-4.899h.613v2.071h2.513v-2.071h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m37.358 21.876-4.957-2.863\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.197 40.834 5.028 2.9M70.197 40.834l5.028 2.9\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(4S,5S)-Phacetoperane"},{"SMILES":"CC(=O)O[C@H](C1=CC=CC=C1)[C@@H]1CCCCN1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.29 70.535\"\u003e\u003crect width=\"100%\" height=\"100%\" fill=\"#fff\"/\u003e\u003cdesc\u003eGenerated by the Chemistry Development Kit (http://github.com/cdk)\u003c/desc\u003e\u003cg stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h82v71H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m27.447.91-.003 15.24\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m28.663 16.854-10.53 6.078M27.445 14.742 16.914 20.82\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m18.133 22.932 5.265-3.039M16.914 20.82l5.266-3.039\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.444 16.15 9.914 5.726\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M40.289 39.012h.7l1.302-11.318h-3.3z\" class=\"bond\"/\u003e\u003cpath d=\"m40.639 39.012-13.2 7.618\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M27.439 46.63 14.238 39M25.001 48.037l-10.764-6.222\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.238 39-13.2 7.617\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 46.617.003 15.249M3.477 48.025l.002 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.041 61.866 13.201 7.63\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.242 69.496 13.2-7.617M14.243 66.681l10.76-6.21\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.439 46.63.003 15.249M40.639 39.012l13.197 7.622M53.836 46.634v15.24M53.836 61.874l13.208 7.62M67.044 69.494l13.208-7.62M80.252 61.874v-15.24M80.252 46.634l-10.055-5.8\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"m53.661 46.331.35.607 10.72-4.647-.841-1.457-.84-1.458z\" class=\"bond\"/\u003e\u003cpath fill=\"#ff0d0d\" stroke=\"none\" d=\"M16.504 23.765q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.31.25-.565.756-.881.506-.315 1.274-.315.732 0 1.232.315.5.31.756.875.256.566.256 1.328m-3.863 0q0 .923.387 1.459.392.529 1.22.529.839 0 1.22-.529.387-.536.387-1.459 0-.929-.387-1.453-.381-.523-1.208-.523-.834 0-1.227.523-.392.524-.392 1.453M42.901 23.769q0 .756-.256 1.328-.256.565-.756.881-.501.315-1.245.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.881t1.274-.316q.732 0 1.233.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.22.53.84 0 1.221-.53.387-.536.387-1.459 0-.928-.387-1.452-.381-.524-1.209-.524-.833 0-1.226.524t-.393 1.452\" class=\"atom\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.985 41.464h-.721l-2.619-4.066h-.03l.03.595q.024.358.024.733v2.738h-.566v-4.899h.715l2.607 4.054h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.768h.578zM68.848 36.003h-.619v-2.286h-2.513v2.286h-.613v-4.899h.613v2.071h2.513v-2.071h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m37.358 21.876-4.957-2.863\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.197 40.834 5.028 2.9M70.197 40.834l5.028 2.9\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(4R,5S)-Phacetoperane"},{"SMILES":"CC(=O)O[C@@H](C1=CC=CC=C1)[C@H]1CCCCN1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.29 70.535\"\u003e\u003crect width=\"100%\" height=\"100%\" fill=\"#fff\"/\u003e\u003cdesc\u003eGenerated by the Chemistry Development Kit (http://github.com/cdk)\u003c/desc\u003e\u003cg fill=\"#ff0d0d\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h82v71H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m27.447.91-.003 15.24\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m28.663 16.854-10.53 6.078M27.445 14.742 16.914 20.82\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m18.133 22.932 5.265-3.039M16.914 20.82l5.266-3.039\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.444 16.15 9.914 5.726\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M40.289 39.012h.7M39.998 36.472h1.283M39.706 33.932h1.867M39.415 31.392h2.45M39.124 28.852h3.033\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M41.865 31.392H40.64M42.157 28.852h-1.516\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m40.639 39.012-13.2 7.618\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M27.439 46.63 14.238 39M25.001 48.037l-10.764-6.222\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.238 39-13.2 7.617\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 46.617.003 15.249M3.477 48.025l.002 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.041 61.866 13.201 7.63\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.242 69.496 13.2-7.617M14.243 66.681l10.76-6.21\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.439 46.63.003 15.249M40.639 39.012l13.197 7.622M53.836 46.634v15.24M53.836 61.874l13.208 7.62M67.044 69.494l13.208-7.62M80.252 61.874v-15.24M80.252 46.634l-10.055-5.8\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m53.661 46.331.35.607M55.423 45.026l.6 1.04M57.185 43.721l.849 1.473M58.947 42.416l1.099 1.906M60.709 41.111l1.349 2.339M62.471 39.805l1.599 2.773\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m62.058 43.45-.675-1.169M64.07 42.578l-.8-1.386M62.471 39.805l.799 1.387\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath stroke=\"none\" d=\"M16.504 23.765q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.31.25-.565.756-.881.506-.315 1.274-.315.732 0 1.232.315.5.31.756.875.256.566.256 1.328m-3.863 0q0 .923.387 1.459.392.529 1.22.529.839 0 1.22-.529.387-.536.387-1.459 0-.929-.387-1.453-.381-.523-1.208-.523-.834 0-1.227.523-.392.524-.392 1.453M42.901 23.769q0 .756-.256 1.328-.256.565-.756.881-.501.315-1.245.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.881t1.274-.316q.732 0 1.233.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.22.53.84 0 1.221-.53.387-.536.387-1.459 0-.928-.387-1.452-.381-.524-1.209-.524-.833 0-1.226.524t-.393 1.452\" class=\"atom\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.985 41.464h-.721l-2.619-4.066h-.03l.03.595q.024.358.024.733v2.738h-.566v-4.899h.715l2.607 4.054h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.768h.578zM68.848 36.003h-.619v-2.286h-2.513v2.286h-.613v-4.899h.613v2.071h2.513v-2.071h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m37.358 21.876-4.957-2.863\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.197 40.834 5.028 2.9M70.197 40.834l5.028 2.9\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(4S,5R)-Phacetoperane"},{"SMILES":"CC(=O)O[C@H](C1=CC=CC=C1)[C@H]1CCCCN1","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.29 70.535\"\u003e\u003crect width=\"100%\" height=\"100%\" fill=\"#fff\"/\u003e\u003cdesc\u003eGenerated by the Chemistry Development Kit (http://github.com/cdk)\u003c/desc\u003e\u003cg fill=\"#ff0d0d\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h82v71H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m27.447.91-.003 15.24\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m28.663 16.854-10.53 6.078M27.445 14.742 16.914 20.82\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m18.133 22.932 5.265-3.039M16.914 20.82l5.266-3.039\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.444 16.15 9.914 5.726\" class=\"bond\"/\u003e\u003cpath fill=\"#000\" stroke=\"none\" d=\"M40.289 39.012h.7l1.302-11.318h-3.3z\" class=\"bond\"/\u003e\u003cpath d=\"m40.639 39.012-13.2 7.618\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M27.439 46.63 14.238 39M25.001 48.037l-10.764-6.222\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.238 39-13.2 7.617\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 46.617.003 15.249M3.477 48.025l.002 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.041 61.866 13.201 7.63\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.242 69.496 13.2-7.617M14.243 66.681l10.76-6.21\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.439 46.63.003 15.249M40.639 39.012l13.197 7.622M53.836 46.634v15.24M53.836 61.874l13.208 7.62M67.044 69.494l13.208-7.62M80.252 61.874v-15.24M80.252 46.634l-10.055-5.8\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m53.661 46.331.35.607M55.423 45.026l.6 1.04M57.185 43.721l.849 1.473M58.947 42.416l1.099 1.906M60.709 41.111l1.349 2.339M62.471 39.805l1.599 2.773\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m62.058 43.45-.675-1.169M64.07 42.578l-.8-1.386M62.471 39.805l.799 1.387\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath stroke=\"none\" d=\"M16.504 23.765q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.31.25-.565.756-.881.506-.315 1.274-.315.732 0 1.232.315.5.31.756.875.256.566.256 1.328m-3.863 0q0 .923.387 1.459.392.529 1.22.529.839 0 1.22-.529.387-.536.387-1.459 0-.929-.387-1.453-.381-.523-1.208-.523-.834 0-1.227.523-.392.524-.392 1.453M42.901 23.769q0 .756-.256 1.328-.256.565-.756.881-.501.315-1.245.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.881t1.274-.316q.732 0 1.233.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.22.53.84 0 1.221-.53.387-.536.387-1.459 0-.928-.387-1.452-.381-.524-1.209-.524-.833 0-1.226.524t-.393 1.452\" class=\"atom\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.985 41.464h-.721l-2.619-4.066h-.03l.03.595q.024.358.024.733v2.738h-.566v-4.899h.715l2.607 4.054h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.768h.578zM68.848 36.003h-.619v-2.286h-2.513v2.286h-.613v-4.899h.613v2.071h2.513v-2.071h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m37.358 21.876-4.957-2.863\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.197 40.834 5.028 2.9M70.197 40.834l5.028 2.9\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Title":"(4R,5R)-Phacetoperane"}],"StereoisomerType":"diastereomer","Stereoisomers":["(4S,5S)-Phacetoperane","(4R,5S)-Phacetoperane","(4S,5R)-Phacetoperane","(4R,5R)-Phacetoperane"],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 81.29 70.535\"\u003e\u003crect width=\"100%\" height=\"100%\" fill=\"#fff\"/\u003e\u003cdesc\u003eGenerated by the Chemistry Development Kit (http://github.com/cdk)\u003c/desc\u003e\u003cg fill=\"#ff0d0d\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h82v71H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m27.447.91-.003 15.24\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m28.663 16.854-10.53 6.078M27.445 14.742 16.914 20.82\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m18.133 22.932 5.265-3.039M16.914 20.82l5.266-3.039\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.444 16.15 9.914 5.726M40.641 27.694l-.002 11.318M40.639 39.012l13.197 7.622M53.836 46.634v15.24M53.836 61.874l13.208 7.62M67.044 69.494l13.208-7.62M80.252 61.874v-15.24M80.252 46.634l-10.055-5.8M53.836 46.634l10.054-5.8M40.639 39.012l-13.2 7.618\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M27.439 46.63 14.238 39M25.001 48.037l-10.764-6.222\"/\u003e\u003c/g\u003e\u003cpath d=\"m14.238 39-13.2 7.617\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m1.038 46.617.003 15.249M3.477 48.025l.002 12.434\"/\u003e\u003c/g\u003e\u003cpath d=\"m1.041 61.866 13.201 7.63\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"m14.242 69.496 13.2-7.617M14.243 66.681l10.76-6.21\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.439 46.63.003 15.249\" class=\"bond\"/\u003e\u003cpath stroke=\"none\" d=\"M16.504 23.765q0 .756-.256 1.328-.256.565-.756.881-.5.315-1.244.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.31.25-.565.756-.881.506-.315 1.274-.315.732 0 1.232.315.5.31.756.875.256.566.256 1.328m-3.863 0q0 .923.387 1.459.392.529 1.22.529.839 0 1.22-.529.387-.536.387-1.459 0-.929-.387-1.453-.381-.523-1.208-.523-.834 0-1.227.523-.392.524-.392 1.453M42.901 23.769q0 .756-.256 1.328-.256.565-.756.881-.501.315-1.245.315-.756 0-1.262-.315-.506-.316-.756-.887-.244-.572-.244-1.334 0-.75.244-1.309.25-.566.756-.881t1.274-.316q.732 0 1.233.316.5.309.756.875.256.565.256 1.327m-3.864 0q0 .923.387 1.459.393.53 1.22.53.84 0 1.221-.53.387-.536.387-1.459 0-.928-.387-1.452-.381-.524-1.209-.524-.833 0-1.226.524t-.393 1.452\" class=\"atom\"/\u003e\u003cg fill=\"#3050f8\" stroke=\"none\" class=\"atom\"\u003e\u003cpath d=\"M68.985 41.464h-.721l-2.619-4.066h-.03l.03.595q.024.358.024.733v2.738h-.566v-4.899h.715l2.607 4.054h.03l-.018-.328-.024-.476q-.006-.262-.006-.482v-2.768h.578zM68.848 36.003h-.619v-2.286h-2.513v2.286h-.613v-4.899h.613v2.071h2.513v-2.071h.619z\"/\u003e\u003c/g\u003e\u003cpath stroke=\"#ff0d0d\" d=\"m37.358 21.876-4.957-2.863M40.641 27.694l-.001 5.659\" class=\"hi\"/\u003e\u003cpath stroke=\"#3050f8\" d=\"m70.197 40.834 5.028 2.9M70.197 40.834l5.028 2.9M63.89 40.834l-5.027 2.9M63.89 40.834l-5.027 2.9\" class=\"hi\"/\u003e\u003c/g\u003e\u003c/g\u003e\u003c/svg\u003e","Subjective Effects":{"Cognitive Effects":["Analysis enhancement","Ego inflation","Focus enhancement","Increased music appreciation","Motivation enhancement","Thought acceleration","Wakefulness","Disinhibition","Suggestibility suppression","Cognitive euphoria","Compulsive redosing","Mania"],"Physical Effects":["Increased libido","Stamina enhancement","Stimulation","Appetite suppression","Dehydration","Dry mouth","Restless legs","Shakiness","Teeth grinding","Abnormal heartbeat","Increased blood pressure","Increased heart rate","Vasoconstriction"],"Visual Effects":[]},"Title":"Phacetoperane","Wikipedia":"Levophacetoperane","XLogP":2.1}
